FDA 510(k) Applications Submitted by Johanna Wright

FDA 510(k) Number Submission Date Device Name Applicant
K170924 03/29/2017 AirFit F20 ResMed Ltd
K153563 12/14/2015 AirFit F20 RESMED LTD.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact